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FDA Inspection
•Allermed Laboratories, Inc.•September 30, 2026

Allermed Laboratories, Inc. – FDA Inspection, Sep 30, 2026

Record Details

This FDA Inspection record concerns Allermed Laboratories, Inc., with an inspection on September 30, 2026, issued by the Los Angeles District Office, covering biologics.

Company
Allermed Laboratories, Inc.
Inspection Date
September 30, 2026
Product Type
Biologics
Office
Los Angeles District Office
Person
  • Alan L. Truong
View Company Profile

ID · 9adf1a05-d729-474c-bf4c-fc7337074c91

Inspection Facts

Inspection number
1338848
FDA center
Biologics
Project area
Vaccines and Allergenic Products
Outcome
Form 483 issued

FDA Citations

5
  1. 21 CFR 211.113(b)Procedures for sterile drug products
  2. 21 CFR 211.22(d)Procedures not in writing, fully followed
  3. 21 CFR 211.42(a)Buildings of Suitable Size, Construction, Location
  4. 21 CFR 211.63Equipment Design, Size and Location
  5. 21 CFR 211.84(d)(2)Component written specification

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Allermed Laboratories, Inc.

7
DateClassificationOfficeProject area
January 31, 2024VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
November 12, 2018VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 14, 2017VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
July 13, 2015VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
August 12, 2013VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
View all 7 other inspections on the company page
Other documents for Allermed Laboratories, Inc.
  • FDA Inspection 1228221 - 2024-01-31
  • FDA Inspection 1071500 - 2018-11-12
  • FDA Inspection 1022877 - 2017-06-14
  • FDA Inspection 933388 - 2015-07-13
  • FDA Inspection 843070 - 2013-08-12

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